Lista de obras - Majid Naderi - Dominio Público Uruguay

A Comparison of Efficacy Between Recombinant Activated Factor VII (Aryoseven) and Novoseven in Patients With Hereditary FVIII Deficiency With Inhibitor.

artículo científico publicado en 2014

A comparison between recombinant activated factor VII (Aryoseven) and Novoseven in patients with congenital factor VII deficiency

artículo científico publicado en 2014

A large case series on surgical outcomes in congenital factor XIII deficiency patients in Iran.

artículo científico publicado en 2017

A prospective study of tubular dysfunction in pediatric patients with Beta thalassemia major receiving deferasirox

artículo científico publicado en 2013

Arg77His and Trp187Arg are the most common mutations causing FXIII deficiency in Iran.

artículo científico

Association between expression of MMP-2 and MMP-9 genes and pathogenesis of intracranial hemorrhage in severe coagulation factor XIII deficiency

artículo científico publicado en 2014

Association of functional polymorphism at the miR-502-binding site in the 3' untranslated region of the SETD8 gene with risk of childhood acute lymphoblastic leukemia, a preliminary report.

artículo científico publicado en 2014

Association of lnc-LAMC2-1:1 rs2147578 and CASC8 rs10505477 Polymorphisms with Risk of Childhood Acute Lymphoblastic Leukemia

artículo científico publicado en 2016

Central nervous system bleeding in pediatric patients with factor XIII deficiency: a study on 23 new cases

artículo científico publicado en 2014

Challenges in implementation of ISTH diagnostic algorithm for diagnosis and classification of factor XIII deficiency in Iran

artículo científico publicado en 2015

Childhood acute lymphoblastic leukemia: refusal and abandonmentof treatment in the southeast of Iran.

artículo científico publicado en 2016

Clinical manifestations and management of life-threatening bleeding in the largest group of patients with severe factor XIII deficiency.

artículo científico publicado en 2014

Coinheritance of Gaucher disease and α-thalassemia resulting in confusion between two inherited hematologic diseases

artículo científico publicado en 2010

Congenital combined deficiency of coagulation factors: a study of seven patients

artículo científico publicado en 2015

Congenital factor V deficiency: comparison of the severity of clinical presentations among patients with rare bleeding disorders

artículo científico publicado en 2014

DROSHA rs642321 Polymorphism Influence Susceptibility to Childhood Acute Lymphoblastic Leukemia: A Preliminary Report

artículo científico publicado en 2017

Diabetes as the cause of end-stage renal disease affects the pattern of post kidney transplant rehospitalizations

artículo científico publicado en 2007

Diagnosis of factor XIII deficiency

artículo científico publicado en 2016

Disseminated intravascular coagulation with positive D-dimer: a controversial clinical feature in severe congenital factor XIII deficiency in southeast Iran.

artículo científico publicado en 2016

Effects of a subdermal levonorgestrel contraceptive implant (Norplant) on serum cholesterol, triglycerides, ALT and AST in Iranian women.

artículo científico publicado en 2005

Establishment of a prenatal diagnosis schedule as part of a prophylaxis program of factor XIII deficiency in the southeast of Iran.

artículo científico publicado en 2016

Evaluation of functional RAGE gene polymorphisms in childhood acute lymphoblastic leukemia-A case-control study from Iran

artículo científico publicado en 2017

Evaluation of the FXIII deficiency prophylaxis intervals in large number of FXIII deficiency patients from Iran.

artículo científico publicado en 2013

Expression and CpG island methylation pattern of MMP-2 and MMP-9 genes in patients with congenital factor XIII deficiency and intracranial hemorrhage

scientific article published on 01 December 2019

FHIT promoter DNA methylation and expression analysis in childhood acute lymphoblastic leukemia

artículo científico publicado en 2017

Factor XIII deficiency diagnosis: Challenges and tools

artículo científico publicado en 2017

Factor XIII deficiency in Iran: a comprehensive review of the literature.

artículo científico publicado en 2015

First cases of severe congenital factor XIII deficiency in Southwestern Afghanistan in the vicinity of southeast of Iran.

artículo científico publicado en 2015

IKZF1 gene polymorphisms increased the risk of childhood acute lymphoblastic leukemia in an Iranian population

scientific article published on 21 January 2016

Intracranial hemorrhage in congenital bleeding disorders

artículo científico publicado en 2017

Intracranial hemorrhage pattern in the patients with factor XIII deficiency

artículo científico publicado en 2013

Long non-coding RNA PAX8-AS1 polymorphisms increase the risk of childhood acute lymphoblastic leukemia

artículo científico publicado en 2017

Long-term prophylaxis in patients with severe congenital factor XIII deficiency is not complicated by inhibitor formation.

artículo científico publicado en 2016

Marital Status and Fertility in Adult Iranian Patients with β-Thalassemia Major.

artículo científico publicado en 2015

Minimal factor XIII activity level to prevent major spontaneous bleeds: comment.

artículo científico publicado en 2017

Miscarriage and recurrent miscarriage in patients with congenital factor V deficiency: a report of six cases in Iran

artículo científico publicado en 2016

Molecular Characterization of β-Thalassemia Intermedia in Southeast Iran

artículo científico publicado en 2016

Molecular basis and prenatal diagnosis of β-thalassemia among Balouch population in Iran

artículo científico publicado en 2011

Molecular characterization of thalassemia intermedia, due to co-inheritance of homozygous alpha triplication and IVSI-5 beta-thalassemia.

artículo científico publicado en 2009

Molecular diagnosis of factor XIII deficiency, data from comprehensive coagulation laboratory in Iran.

artículo científico publicado en 2017

Molecular genetic analysis of ten unrelated Iranian patients with congenital factor XIII deficiency.

artículo científico publicado en 2016

Morbidity and mortality in a large number of Iranian patients with severe congenital factor XIII deficiency.

artículo científico

Polymorphism of thrombin-activatable fibrinolysis inhibitor and risk of intracranial haemorrhage in factor XIII deficiency.

artículo científico publicado en 2013

Post-traumatic stress disorder and related factors in parents of children with cancer in South-East of iran

artículo científico publicado en 2012

Pri-miR-34b/c rs4938723 polymorphism is associated with the risk of childhood acute lymphoblastic leukemia

artículo científico publicado en 2016

Prolonged rehospitalizations following renal transplantation: causes, risk factors, and outcomes

scientific article published on 01 May 2007

The burden and management of FXIII deficiency

artículo científico

Lista de obras de Majid Naderi

A Comparison of Efficacy Between Recombinant Activated Factor VII (Aryoseven) and Novoseven in Patients With Hereditary FVIII Deficiency With Inhibitor.

A comparison between recombinant activated factor VII (Aryoseven) and Novoseven in patients with congenital factor VII deficiency

A large case series on surgical outcomes in congenital factor XIII deficiency patients in Iran.

A prospective study of tubular dysfunction in pediatric patients with Beta thalassemia major receiving deferasirox

Arg77His and Trp187Arg are the most common mutations causing FXIII deficiency in Iran.

Association between expression of MMP-2 and MMP-9 genes and pathogenesis of intracranial hemorrhage in severe coagulation factor XIII deficiency

Association of functional polymorphism at the miR-502-binding site in the 3' untranslated region of the SETD8 gene with risk of childhood acute lymphoblastic leukemia, a preliminary report.

Association of lnc-LAMC2-1:1 rs2147578 and CASC8 rs10505477 Polymorphisms with Risk of Childhood Acute Lymphoblastic Leukemia

Central nervous system bleeding in pediatric patients with factor XIII deficiency: a study on 23 new cases

Challenges in implementation of ISTH diagnostic algorithm for diagnosis and classification of factor XIII deficiency in Iran

Childhood acute lymphoblastic leukemia: refusal and abandonmentof treatment in the southeast of Iran.

Clinical manifestations and management of life-threatening bleeding in the largest group of patients with severe factor XIII deficiency.

Coinheritance of Gaucher disease and α-thalassemia resulting in confusion between two inherited hematologic diseases

Congenital combined deficiency of coagulation factors: a study of seven patients

Congenital factor V deficiency: comparison of the severity of clinical presentations among patients with rare bleeding disorders

DROSHA rs642321 Polymorphism Influence Susceptibility to Childhood Acute Lymphoblastic Leukemia: A Preliminary Report

Diabetes as the cause of end-stage renal disease affects the pattern of post kidney transplant rehospitalizations

Diagnosis of factor XIII deficiency

Disseminated intravascular coagulation with positive D-dimer: a controversial clinical feature in severe congenital factor XIII deficiency in southeast Iran.

Effects of a subdermal levonorgestrel contraceptive implant (Norplant) on serum cholesterol, triglycerides, ALT and AST in Iranian women.

Establishment of a prenatal diagnosis schedule as part of a prophylaxis program of factor XIII deficiency in the southeast of Iran.

Evaluation of functional RAGE gene polymorphisms in childhood acute lymphoblastic leukemia-A case-control study from Iran

Evaluation of the FXIII deficiency prophylaxis intervals in large number of FXIII deficiency patients from Iran.

Expression and CpG island methylation pattern of MMP-2 and MMP-9 genes in patients with congenital factor XIII deficiency and intracranial hemorrhage

FHIT promoter DNA methylation and expression analysis in childhood acute lymphoblastic leukemia

Factor XIII deficiency diagnosis: Challenges and tools

Factor XIII deficiency in Iran: a comprehensive review of the literature.

First cases of severe congenital factor XIII deficiency in Southwestern Afghanistan in the vicinity of southeast of Iran.

IKZF1 gene polymorphisms increased the risk of childhood acute lymphoblastic leukemia in an Iranian population

Intracranial hemorrhage in congenital bleeding disorders

Intracranial hemorrhage pattern in the patients with factor XIII deficiency

Long non-coding RNA PAX8-AS1 polymorphisms increase the risk of childhood acute lymphoblastic leukemia

Long-term prophylaxis in patients with severe congenital factor XIII deficiency is not complicated by inhibitor formation.

Marital Status and Fertility in Adult Iranian Patients with β-Thalassemia Major.

Minimal factor XIII activity level to prevent major spontaneous bleeds: comment.

Miscarriage and recurrent miscarriage in patients with congenital factor V deficiency: a report of six cases in Iran

Molecular Characterization of β-Thalassemia Intermedia in Southeast Iran

Molecular basis and prenatal diagnosis of β-thalassemia among Balouch population in Iran

Molecular characterization of thalassemia intermedia, due to co-inheritance of homozygous alpha triplication and IVSI-5 beta-thalassemia.

Molecular diagnosis of factor XIII deficiency, data from comprehensive coagulation laboratory in Iran.

Molecular genetic analysis of ten unrelated Iranian patients with congenital factor XIII deficiency.

Morbidity and mortality in a large number of Iranian patients with severe congenital factor XIII deficiency.

Polymorphism of thrombin-activatable fibrinolysis inhibitor and risk of intracranial haemorrhage in factor XIII deficiency.

Post-traumatic stress disorder and related factors in parents of children with cancer in South-East of iran

Pri-miR-34b/c rs4938723 polymorphism is associated with the risk of childhood acute lymphoblastic leukemia

Prolonged rehospitalizations following renal transplantation: causes, risk factors, and outcomes

The burden and management of FXIII deficiency